Structure of PDB 6v2m Chain A Binding Site BS01
Receptor Information
>6v2m Chain A (length=531) Species:
562
(Escherichia coli) [
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EELEAYGISDVHDIVYNPSYDLLYQEELDPSLTGYERGVLTNLGAVAVDT
GIFTGRSPKDKYIVRDDTTRDTFWWADKGKGKNDNKPLSPETWQHLKGLV
TRQLSGKRLFVVDAFCGANPDTRLSVRFITEVAWQAHFVKNMFIRPSDEE
LAGFKPDFIVMNGAKCTNPQWKEQGLNSENFVAFNLTERMQLIGGTWYGG
EMKKGMFSMMNYLLPLKGIASMHCSANVGEKGDVAVFFGLSGTGKTTLST
DPKRRLIGDNEHGWDDDGVFNFEGGCYAKTIKLSKEAEPEIYNAIRRDAL
LENVTKREDGTIDFDDGSKTENTRVSYPIYHIDNIVKPVSKAGHATKVIF
LTADAFGVLPPVSRLTADQTQYHFLSGFTAKLAGTERGITEPTPTFSACF
GAAFLSLHPTQYAEVLVKRMQAAGAQAYLVNTGWNGTGKRISIKDTRAII
DAILNGSLDNAETFTLPMFNLAIPTELPGVDTKILDPRNTYASPEQWQEK
AETLAKLFIDNFDKYTDTPAGAALVAAGPKL
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
6v2m Chain A Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
6v2m
Kinetic and structural analysis of Escherichia coli phosphoenolpyruvate carboxykinase mutants.
Resolution
1.66 Å
Binding residue
(original residue number in PDB)
S250 G251 G253 K254 T255 T256 K288 R333 R449 I452 T455
Binding residue
(residue number reindexed from 1)
S241 G242 G244 K245 T246 T247 K279 R324 R440 I443 T446
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
R65 K213 H232 S250 K254 T255 N269 R333
Catalytic site (residue number reindexed from 1)
R56 K204 H223 S241 K245 T246 N260 R324
Enzyme Commision number
4.1.1.49
: phosphoenolpyruvate carboxykinase (ATP).
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004611
phosphoenolpyruvate carboxykinase activity
GO:0004612
phosphoenolpyruvate carboxykinase (ATP) activity
GO:0005509
calcium ion binding
GO:0005524
ATP binding
GO:0016831
carboxy-lyase activity
GO:0017076
purine nucleotide binding
GO:0046872
metal ion binding
Biological Process
GO:0006094
gluconeogenesis
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6v2m
,
PDBe:6v2m
,
PDBj:6v2m
PDBsum
6v2m
PubMed
31911238
UniProt
P22259
|PCKA_ECOLI Phosphoenolpyruvate carboxykinase (ATP) (Gene Name=pckA)
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